Cardiac Amyloidosis: Clinical Features, Pathogenesis, Diagnosis, and Treatment

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dc.authoridYılmaz, Funda/0000-0003-1837-6498
dc.authoridNART, DENIZ/0000-0002-8100-6978
dc.contributor.authorArgon, Asuman
dc.contributor.authorNart, Deniz
dc.contributor.authorBarbet, Funda Y. I. L. M. A. Z.
dc.date.accessioned2024-08-31T07:46:40Z
dc.date.available2024-08-31T07:46:40Z
dc.date.issued2024
dc.departmentEge Üniversitesien_US
dc.description.abstractCardiac amyloidosis is a type of amyloidosis that deserves special attention as organ involvement significantly worsens the prognosis. Cardiac amyloidosis can be grouped under three main headings: immunoglobulin light chain (AL) amyloidosis that is dependent on amyloidogenic monoclonal light chain production; hereditary Transthyretin (TTR) amyloidosis that results from accumulation of mutated TTR; and wild-type (non-hereditary) TTR amyloidosis formerly known as senile amyloidosis. Although all three types cause morbidity and mortality due to severe heart failure when untreated, they contain differences in their pathogenesis, clinical findings, and treatment. In this article, the clinical features, pathogenesis, diagnosis, and treatment methods of cardiac amyloidosis will be explained with an overview, and an awareness will be raised in the diagnosis of this disease.en_US
dc.identifier.doi10.5146/tjpath.2023.12923
dc.identifier.endpage9en_US
dc.identifier.issn1018-5615
dc.identifier.issn1309-5730
dc.identifier.issue1en_US
dc.identifier.pmid38111336en_US
dc.identifier.scopus2-s2.0-85182956913en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage1en_US
dc.identifier.trdizinid1251985en_US
dc.identifier.urihttps://doi.org/10.5146/tjpath.2023.12923
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1251985
dc.identifier.urihttps://hdl.handle.net/11454/104167
dc.identifier.volume40en_US
dc.identifier.wosWOS:001157776000001en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherFederation Turkish Pathology Socen_US
dc.relation.ispartofTurkish Journal of Pathologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.snmz20240831_Uen_US
dc.subjectAmyloiden_US
dc.subjectCardiac Amyloidosisen_US
dc.subjectTransthyretinen_US
dc.subjectHereditary Amyloidosisen_US
dc.subjectSenile Amyloidosisen_US
dc.titleCardiac Amyloidosis: Clinical Features, Pathogenesis, Diagnosis, and Treatmenten_US
dc.typeReview Articleen_US

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